Addition of indoles to N-alkylpyridinium salts. Synthesis of (dihydropyridyl)indoles
- Author
- ALVAREZ, M1 ; LAVILLA, R; BOSCH, J
[1] Univ. Barcelona, fac. pharmacy, lab. organic chemistry, Barcelona 08028, Spain - Source
Heterocycles (Sendai). 1989, Vol 29, Num 2, pp 237-242 ; ref : 17 ref
- CODEN
- HTCYAM
- ISSN
- 0385-5414
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition chimique Carbanion Cation organique Composé aromatique Composé bicyclique Cycle 6 chaînons Hétérocycle azote Iminium composé Spectre RMN Spectrométrie 2 dimensions Carbone 13 Indoleacétique-2 acide([dihydro-1,2 méthoxycarbonyl-«2p» vinyl-«5» méthyl-«1» pyridyl-«2»]-«3») ester méthyle Indolure-3 dérivé Pyridineacrylique-3 acide dérivé Pyridinium composé
- Keyword (en)
- Addition reaction Carbanion Organic cation Aromatic compound Bicyclic compound Six membered ring Nitrogen heterocycle Iminium compounds NMR spectrum Two dimension spectrometry
- Keyword (es)
- Adición química Carbanión Catión orgánico Compuesto aromático Compuesto bicíclico Ciclo 6 eslabones Heterociclo nitrógeno Iminio compuesto Espectro de RMN Espectrometría bidimensional
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 6954123
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.3987/COM-89-4799 
https://dx.doi.org/10.3987/COM-89-4799
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